US9127116B2ActiveUtilityA1
Functional silane-compatibilized epoxy compositions for insulation applications
Est. expiryDec 30, 2031(~5.5 yrs left)· nominal 20-yr term from priority
C07F 7/081C08L 63/00C08G 59/42C08K 5/5419C08G 59/24C08G 59/4085C08K 5/09C08G 77/16C08L 83/04
69
PatentIndex Score
2
Cited by
22
References
14
Claims
Abstract
Described is an epoxy composition containing: (a) an epoxy resin containing at least one epoxy group, (b) an anhydride hardener, (c) a hydroxyl-terminated polysiloxane, and (d) a functional silane having at least one functional group selected from the group consisting of an epoxy-reactive group, an anhydride-reactive group, and an epoxy- and anhydride-reactive group. Also describing a crosslinked epoxy composition and a method for preparing thereof.
Claims
exact text as granted — not AI-modifiedThe invention claimed is:
1. An epoxy composition comprising:
(a) an epoxy resin containing at least one epoxy group,
(b) an anhydride hardener,
(c) a hydroxyl-terminated polysiloxane, and
(d) a functional silane having at least one functional group selected from the group consisting of an epoxy-reactive group, an anhydride-reactive group, and an epoxy- and anhydride-reactive group, wherein molar ratio of the functional group of the functional silane to the epoxy group of the epoxy resin (a) is less than 0.25;
wherein molar ratio of total hydroxyl group(s) in the hydroxyl-terminated polysiloxane to total alkoxy group(s) in the functional silane is 3.5 or less.
2. The epoxy composition of claim 1 , wherein the epoxy resin is a cycloaliphatic epoxy resin.
3. The epoxy composition of claim 1 , wherein the molar ratio of total hydroxyl group(s) in the hydroxyl-terminated polysiloxane to total alkoxy group(s) in the functional silane is from 0.001 to 1.5.
4. The epoxy composition of claim 1 , wherein the functional silane is selected from an aminosilane and an epoxy silane.
5. The epoxy composition of claim 1 , wherein the hydroxyl-terminated polysiloxane is hydroxyl-terminated polydimethylsiloxane.
6. The epoxy composition of claim 1 , wherein the content of the hydroxyl-terminated polysiloxane is from 0.5 to 25 weight-percent based on the weight of the epoxy resin.
7. The epoxy composition of claim 1 , wherein molecular weight of the hydroxyl-terminated polysiloxane is from 400 grams per mole to 70,000 grams per mole.
8. The epoxy composition of claim 1 further comprising a cyclic polysiloxane.
9. The epoxy composition of claim 8 , wherein the content of the cyclic polysiloxane is from one to 3 weight-percent, based on the epoxy resin weight.
10. A crosslinked epoxy composition obtained by curing the epoxy composition of any of claims 1 - 9 .
11. A method for preparing the epoxy composition of claim 1 , comprising steps of mixing
(a) an epoxy resin containing at least one epoxy group,
(b) an anhydride hardener,
(c) a hydroxyl-terminated polysiloxane, and
(d) a functional silane having at least one functional group selected from the group consisting of an epoxy-reactive group, an anhydride-reactive group, and an epoxy- and anhydride-reactive group, wherein molar ratio of the functional group of the functional silane to the epoxy group of the epoxy resin (a) is less than 0.25;
wherein molar ratio of total hydroxyl group(s) in the hydroxyl-terminated polysiloxane to total alkoxy group(s) in the functional silane is 3.5 or less.
12. The method of claim 11 , wherein the anhydride hardener, the hydroxyl-terminated polysiloxane and the functional silane are mixed to react first, before mixing with the epoxy resin.
13. The method of claim 11 , wherein the epoxy resin, the hydroxyl-terminated polysiloxane and the functional silane are mixed to react first, before mixing with the anhydride hardener.
14. The method of claim 13 , wherein the epoxy resin reacts with the functional silane having at least one epoxy-reactive group or at least one epoxy- and anhydride-reactive group first, before mixing with the hydroxyl-terminated polysiloxane.Cited by (0)
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